ライフサイエンスコーパス: enterochromaffin cell

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1 icate goblet cells, whereas others implicate enterochromaffin cells).

2 e adult stage in a subset of enteroendocrine/enterochromaffin cells.

3 by 5-hydroxytryptamine (5-HT) released from enterochromaffin cells.

4 g cells are identified as a subpopulation of enterochromaffin cells.

5 in neuroendocrine, including chromaffin and enterochromaffin, cells.

6 onstrated that 5-HT released from intestinal enterochromaffin cells activates 5-HT3 receptors on vaga

7 5-Hydroxytryptamine (5-HT) released from enterochromaffin cells activates secretory and peristalt

8 5-Hydroxytryptamine (5-HT) is released from enterochromaffin cells and activates neural reflex progr

9 e of 5-hydroxytryptamine (5-HT) from mucosal enterochromaffin cells and activation of 5-HT(3) recepto

10 e transcription factor Lmx1a is expressed in enterochromaffin cells and functions downstream of Nkx2.

11 Serotonin is also released from enterochromaffin cells and inflammatory/immune cells to

12 sis, consistent with localization of TGR5 to enterochromaffin cells and intrinsic primary afferent ne

13 med FFA2 and FFA3, are expressed in duodenal enterochromaffin cells and L cells, respectively.

14 ivity was abundant in both enteric plexuses, enterochromaffin cells, and pancreatic ganglia.

15 release serotonin (5-hydroxytryptamine) from enterochromaffin cells, and stretch reflexes that determ

16 vious results showing guanylin expression in enterochromaffin cells appear to be a consequence of ant

17 These findings imply a role for enterochromaffin cells as "glucose sensors" during inges

18 We show that the number of mucosal enterochromaffin cells containing 5-HT changes with the

19 Paracrine signaling by enterochromaffin cells (EC), which release 5-HT, has not

20 biota promote 5-HT biosynthesis from colonic enterochromaffin cells (ECs), which supply 5-HT to the m

21 tion to neurons, a subset of 5-HT-containing enterochromaffin cells expressed 5-HT1A immunoreactivity

22 Mucosal enterochromaffin cells have been postulated to be pressu

23 onsistent with the hypothesis that 5-HT from enterochromaffin cells in response to mucosal stimuli in

24 neurons were activated by 5-HT release from enterochromaffin cells in the mucosa.

25 5-HT released from enterochromaffin cells initiates peristaltic, secretory,

26 Expression of uroguanylin in enterochromaffin cells is consistent with the hypothesis

27 5HT produced by enterochromaffin cells is critical in motility and secre

28 g kg-1) indicating that endogenous 5-HT from enterochromaffin cells is not essential for transduction

29 erotonin (5-HT), which abounds in intestinal enterochromaffin cells, is released in response to vario

30 e populations, and identify Lmx1a as a novel enterochromaffin cell marker that is also essential for

31 athematical modeling, we show that, in human enterochromaffin cells, Myrip (1) inhibits a class of SG

32 imiting biosynthetic enzyme for serotonin in enterochromaffin cells of the duodenum.

33 a decrease in the synthesis of serotonin by enterochromaffin cells of the gut.

34 , it is unclear whether they act directly on enterochromaffin cells or indirectly through an intermed

35 The enterochromaffin cell population was decreased in severe

36 er RNA, encoding the rate-limiting enzyme in enterochromaffin cell serotonin (5-hydroxytryptamine [5H

37 kx2.2 mutant conditions, serotonin-producing enterochromaffin cells were the most severely reduced en

38 Human BON cells, derived from enterochromaffin cells, were treated with D-glucose, gal

39 release of endogenous 5-HT from the mucosal enterochromaffin cells, which acts on the 5-HT3 receptor

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